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Geology topics

James R. Hein

Publications and source records attributed to James R. Hein.

At least 73 records · Page 4Linked to original sources
USGS2002

Genesis of the Doğankuzu and Mortaş Bauxite deposits, Taurides, Turkey: separation of Al, Fe, and Mn and implications for passive margin metallogeny

The Taurides region of Turkey is host to a number of important bauxite, Al-rich laterite, and Mn deposits. The most important bauxite deposits, Doğankuzu and Mortaş, are karst-related, unconformity-type deposits in Upper Cretaceous limestone. The bottom contact of the bauxite ore is undulatory, and bauxite fills depressions and sinkholes in the footwall limestone, whereas its top surface is concordant with the hanging-wall limestone. The thickness of the bauxite varies from 1 to 40 m and consists of böhmite, hematite, pyrite, marcasite, anatase, diaspore, gypsum, kaolinite, and smectite. The strata-bound, sulfide- and sulfate-bearing, low-grade lower part of the bauxite ore bed contains pyrite pseudomorphs after hematite and is deep red in outcrop owing to supergene oxidation. The lower part of the bauxite body contains local intercalations of calcareous conglomerate that formed in fault-controlled depressions and sinkholes. Bauxite ore is overlain by fine-grained Fe sulfide-bearing and calcareous claystone and argillaceous limestone, which are in turn overlain by massive, compact limestone of Santonian age. That 50-m-thick limestone is in turn overlain by well-bedded bioclastic limestone of Campanian or Maastrichtian age, rich with rudist fossils. Fracture fillings in the bauxite orebody are up to 1 m thick and consist of bluish-gray-green pyrite and marcasite (20%) with böhmite, diaspore, and anatase. These sulfide veins crosscut and offset the strata-bound sulfide zones. Sulfur for the sulfides was derived from the bacterial reduction of seawater sulfate, and Fe was derived from alteration of oxides in the bauxite. Iron sulfides do not occur within either the immediately underlying or overlying limestone. The platform limestone and shale that host the bauxite deposits formed at a passive margin of the Tethys Ocean. Extensive vegetation developed on land as the result of a humid climate, thereby creating thick and acidic soils and enhancing the transport of large amounts of organic matter to the ocean. Alteration of the organic matter provided CO 2 that contributed to formation of a relatively 12 C-rich marine footwall limestone. Relative sea-level fall resulted from strike-slip faulting associated with closure of the ocean and local uplift of the passive margin. That uplift resulted in karstification and bauxite formation in topographic lows, as represented by the Doğankuzu and Mortaş deposits. During stage 1 of bauxite formation, Al, Fe, Mn, and Ti were mobilized from deeply weathered aluminosilicate parent rock under acidic conditions and accumulated as hydroxides at the limestone surface owing to an increase in pH. During stage 2, Al, Fe, and Ti oxides and clays from the incipient bauxite (bauxitic soil) were transported as detrital phases and accumulated in the fault-controlled depressions and sinkholes. During stage 3, the bauxitic material was concentrated by repeated desilicification, which resulted in the transport of Si and Mn to the ocean through a well-developed karst drainage system. The transported Mn was deposited in offshore muds as Mn carbonates. The sulfides also formed in stage 3 during early diagenesis. Transgression into the foreland basin resulted from shortening of the ocean basin and nappe emplacement during the latest Cretaceous. During that time bioclastic limestone was deposited on the nappe ramp, which overlapped bauxite accumulation.

Taurides Region↗
USGS2002

Composition of the Rex Chert and associated rocks of the Permian Phosphoria Formation: Soda Springs area, SE Idaho

This study, one in a series, reports bulk chemical and mineralogical compositions, as well as petrographic and outcrop descriptions of rocks collected from three measured outcrop sections of the Rex Chert member of the Phosphoria Formation in SE Idaho. The three measured sections were chosen from ten outcrops of Rex Chert that were described in the field. The Rex Chert overlies the Meade Peak Phosphatic Shale Member of the Phosphoria Formation, the source of phosphate ore in the region. Rex Chert removed as overburden comprises part of the material disposed in waste-rock piles during phosphate mining. It has been proposed that the chert be used to cap and isolate waste piles, thereby inhibiting the leaching of potentially toxic elements into the environment. It is also used to surface roads in the mining district. The rock samples studied here constitute a set of individual chert beds that are representative of each stratigraphic section sampled. The informally named cherty shale member that overlies the Rex Chert in measured section 1 was also described and sampled. The upper Meade Peak and the transition zone to the Rex Chert were described and sampled in section 7. The cherts are predominantly spicularite composed of granular and mosaic quartz, and sponge spicules, with various but minor amounts of other fossils and detrital grains. The cherty shale member and transition rocks between the Meade Peak and Rex Chert are siliceous siltstones and argillaceous cherts with ghosts of sponge spicules and somewhat more detrital grains than the chert. The overwhelmingly dominant mineral is quartz, although carbonate beds are rare in each section and are composed predominantly of calcite and dolomite in addition to quartz. Feldspar, mica, clay minerals, calcite, dolomite, and carbonate fluorapatite are minor to trace minerals in the chert. The mean concentrations of oxides and elements in the Rex Chert and the cherty shale member are dominated by SiO2, which averages 94.6%. Organic-carbon contents are generally very low in the chert, but are up to 1.8 wt. % in cherty shale member samples and up to 3.3% in samples from the transition between the Meade Peak and Rex Chert. Likewise, phosphate (P2O5) is generally low in the chert, but can be up to 3.1% in individual beds. Selenium concentrations in Rex Chert and cherty shale member samples vary from <0.2 to 138 ppm, with a mean concentration of 7.0 ppm. This mean Se content is heavily dependent on two values of 101 and 138 ppm for rocks from the transition zone between the Meade Peak and Rex Chert. Without those two samples, the mean Se concentration would be <1.0 ppm. Other elements of environmental interest, As, Cr, V, Zn, Hg, and Cd, are generally near or below their content in average continental shale. Stratigraphic changes (equivalent to temporal changes in the depositional basin) in chemical composition of rocks are notable either as uniform changes through the sections or as distinct differences in the mean composition of rocks that compose the upper and lower halves of the sections. Q-mode factors are interpreted to represent the following rock and mineral components: chert-silica component consisting of Si (± Ba); phosphorite-phosphate component composed of P, Ca, As, Y, V, Cr, Sr, and La (± Fe, Zn, Cu, Ni, Li, Se, Nd, Hg); shale component composed of Al, Na, Zr, K, Ba, Li, and organic C (± Ti, Mg, Se, Ni, Fe, Sr, V, Mn, Zn); carbonate component (dolomite, calcite, silicified carbonates) composed of carbonate C, Mg, Ca, and Si (± Mn); tentatively organic matter-hosted elements (and/or sulfide-sulfate phases) composed of Cu (± organic C, Zn, Mn Si, Ni, Hg, and Li). Selenium shows a dominant association with the shale component, but correlations and Qmode factors also indicate that organic matter (within the shale component) and carbonate fluorapatite may host a portion of the Se. Consideration of larger numbers of factors in Qmode analysis indicates that native Se (a factor containing Se (± Ba)) may also comprise a minor component of the Se compliment.

Idaho↗
USGS2001

Clay mineral content of continental shelf and river sediments, southern California

This report contains data on the clay mineral content of 250 shelf surface-sediment samples from the California Continental Borderland (Tables 1, 2; Figures 1-7), 79 samples with depth in cores from Santa Monica Bay (Table 3; see Table 1 for surface sediment data for those same cores and for core locations), 24 suspended and 13 bottom sediment samples from rivers draining Southern California (Table 4), and six rock samples or composite rock samples from the Palos Verdes Headland (Table 4). This report is designed as the data repository and these data are discussed in a paper by Hein et al. (2001).

California↗
USGS2000

Changes in erosion and ocean circulation recorded in the Hf isotopic compositions of North Atlantic and Indian Ocean ferromanganese crusts

High-resolution Hf isotopic records are presented for hydrogenetic Fe–Mn crusts from the North Atlantic and Indian Oceans. BM1969 from the western North Atlantic has previously been shown to record systematically decreasing Nd isotopic compositions from about 60 to ∼4 Ma, at which time both show a rapid decrease to unradiogenic Nd composition, thought to be related to the increasing influence of NADW or glaciation in the northern hemisphere. During the Oligocene, North Atlantic Hf became progressively less radiogenic until in the mid-Miocene (∼15 Ma) it reached +1. It then shifted gradually back to an ϵ Hf value of +3 at 4 Ma, since when it has decreased rapidly to about −1 at the present day. The observed shifts in the Hf isotopic composition were probably caused by variation in intensity of erosion as glaciation progressed in the northern hemisphere. Ferromanganese crusts SS663 and 109D are from about 5500 m depth in the Indian Ocean and are now separated by ∼2300 km across the Mid-Indian Ridge. They display similar trends in Hf isotopic composition from 20 to 5 Ma, with the more northern crust having a composition that is consistently more radiogenic (by ∼2 ϵ Hf units). Paradoxically, during the last 20 Ma the Hf isotopic compositions of the two crusts have converged despite increased separation and subsidence relative to the ridge. A correlatable negative excursion at ∼5 Ma in the two records may reflect a short-term increase in erosion caused by the activation of the Himalayan main central thrust. Changes to unradiogenic Hf in the central Indian Ocean after 5 Ma may alternatively have been caused by the expanding influence of NADW into the Mid-Indian Basin via circum-Antarctic deep water or a reduction of Pacific flow through the Indonesian gateway. In either case, these results illustrate the utility of the Hf isotope system as a tracer of paleoceanographic changes, capable of responding to subtle changes in erosional regime not readily resolved using other isotope systems.

Earth and Planetary Science Letters↗
USGS1999

Stable isotope, chemical, and mineral compositions of the Middle Proterozoic Lijiaying Mn deposit, Shaanxi Province, China

The Lijiaying Mn deposit, located about 250 km southwest of Xian, is a high-quality ore characterized by low P and Fe contents and a mean Mn content of about 23%. The ore deposit occurs in shallow-water marine sedimentary rocks of probable Middle Proterozoic age. Carbonate minerals in the ore deposit include kutnahorite, calcite, Mn calcite, and Mg calcite. Carbon (−0.4 to −4.0‰) and oxygen (−3.7 to −12.9‰) isotopes show that, with a few exceptions, those carbonate minerals are not pristine low-temperature marine precipitates. All samples are depleted in rare earth elements (REEs) relative to shale and have negative Eu and positive Ce anomalies on chondrite-normalized plots. The Fe/Mn ratios of representative ore samples range from about 0.034 to <0.008 and P/Mn from 0.0023 to <0.001. Based on mineralogical data, the low ends of those ranges of ratios are probably close to ratios for the pure Mn minerals. Manganese contents have a strong positive correlation with Ce anomaly values and a moderate correlation with total REE contents. Compositional data indicate that kutnahorite is a metamorphic mineral and that most calcites formed as low-temperature marine carbonates that were subsequently metamorphosed. The braunite ore precursor mineral was probably a Mn oxyhydroxide, similar to those that formed on the deep ocean-floor during the Cenozoic. Because the Lijiaying precursor mineral formed in a shallow-water marine environment, the atmospheric oxygen content during the Middle Proterozoic may have been lower than it has been during the Cenozoic.

Ore Geology Reviews↗
USGS1999

Ordovician reef-hosted Jiaodingshan Mn-Co deposit and Dawashan Mn deposit, Sichuan Province, China

The Jiaodingshan Mn-Co and Dawashan Mn deposits are located in the approximately 2-m thick Daduhe unit of the Wufengian strata of Late Ordovician (Ashgill) age. Paleogeographic reconstruction places the deposits at the time of their formation in a gulf between Chengdu submarine rise and the Kangdian continent. The Jiaodingshan and Dawashan deposits occur in algal-reef facies, the former in an atoll-like structure and the latter in a pinnacle reef. Ores are mainly composed of rhodochrosite, kutnahorite, hausmannite, braunite, manganosite, and bementite. Dark red, yellowish-pink, brown, green-gray, and black ores are massive, banded, laminated, spheroidal, and cryptalgal (oncolite, stromatolite, algal filaments) boundstones. Blue, green, and red algal fossils show in situ growth positions. Samples of high-grade Jiaodingshan and Dawashan ores assay as much as 66.7% MnO. Jiaodingshan Mn carbonate ores have mean contents of Ba, Co, and Pb somewhat higher than in Dawashan ores. Cobalt is widely distributed and strongly enriched in all rock types as compared to its crustal mean content. Cobalt is correlated with Cu, Ni, and MgO in both deposits and additionally with Ba and Zn in the Dawashan deposit. The δ 13 C(PDB) values of Mn carbonate ores (-7.8 to -16.3‰) indicate contributions of carbon from both seawater bicarbonate and the bacterial degradation of organic matter, the latter being 33% to 68%, assuming about -24‰ for the δ 13 C(PDB) of the organic matter. Host limestones derived carbon predominantly from seawater bicarbonate δ 13 13C(PDB) of +0.2 to -7‰). NW-trending fault zones controlled development of lithofacies, whereas NE-trending fault zones provided pathways for movement of fluids. The source of Co, Ni, and Cu was mainly from weathering of mafic and ultramafic rocks on the Kangdian continent, whereas contemporaneous volcanic eruptions were of secondary importance. The reefs were likely mineralized during early diagenesis under shallow burial. The reefs were highly porous and acted as the locus for metasomatic replacement by Mn that combined with CO 2 produced during oxidation of organic matter in the zone of sulfate reduction and seawater bicarbonate. That metasomatic replacement formed the rhodochrosite ores.

Ore Geology Reviews↗
USGS1999

Bathymetry of the Republic of the Marshall Islands and vicinity

The bathymetric map of the Republic of the Marshall Islands and vicinity is bounded by a window of latitude 3 to 17 degrees North, longitude 153 to 175 degrees East. The map was compiled from surveys conducted by the USGS, Korean Ocean Research and Development Institute, and published gridded data. In addition to national jurisdictions, island and atoll coastlines are indicated on the map.

Miscellaneous Field Studies Map↗
USGS1999

Cobalt-rich ferromanganese crusts in the Pacific

Co-rich Fe-Mn crusts occur throughout the Pacific on seamounts, ridges, and plateaus where currents have kept the rocks swept clean of sediments at least intermittently for millions of years. Crusts precipitate out of cold ambient sea water onto hard-rock substrates forming pavements up to 250 mm thick. Crusts are important as a potential resource for Co, Ni, Pt, Mn, Tl, Te, and other metals, as well as for the paleoclimate signals stored in their stratigraphic layers. Crusts form at water depths of about 400 to 4000 m, with the thickest and most Co-rich crusts occurring at depths of about 800 to 2500 m, which may vary on a regional scale. Gravity processes, sediment cover, submerged and emergent reefs, and currents control the distribution and thickness of crusts on seamounts. Crusts occur on a variety of substrate rocks that generally decrease in the order, breccia, basalt, phosphorite, limestone, hyaloclastite, and mudstone. Because of this wide variety of substrate types, crusts are difficult to distinguish from the substrate using remotely sensed data, such as geophysical measurements, but are generally weaker and lighter-weight than the substrate. Crusts can be distinguished from the substrates, however, by their much higher gamma radiation levels. The mean dry bulk density of crusts is 1.3 g/cm3, the mean porosity is 60%, and the mean surface area is extremely high, 300 m2/g. Crusts generally grow at rates of 1 to 10 mm/Ma. Crust surfaces are botryoidal, which may be modified to a variety of forms by current erosion. In cross-section, crusts are generally layered, with individual layers displaying massive, botryoidal, laminated, columnar, or mottled textures. Characteristic layering is persistent regionally in the Pacific. Crusts are composed of ferruginous vernadite (δ-MnO2) and X-ray amorphous Fe oxyhydroxide, with moderate amounts of carbonate fluorapatite (CFA) in thick crusts and minor amounts of quartz and feldspar in most crusts. Elements most commonly associated with the vernadite phase include Mn, Co, Ni, Cd, and Mo, whereas those most commonly associated with Fe oxyhydroxide are Fe and As. Detrital phases are represented by Si, Al, K, Ti, Cr, Mg, Fe, and Na; the CFA phase by Ca, P, Sr, Y, and CO2; and a residual biogenic phase by Ba, Sr, Ce, Cu, V, Ca, and Mg. Crusts contain Co contents up to about 2.3%, Ni to 1%, and Pt to 3 ppm, with mean Fe/Mn ratios of 0.6 to 1.3. Fe/Mn decreases, whereas Co, Ni, Ti, and Pt increase in central Pacific crusts and Fe/Mn, Si, and Al increase in continental margin crusts and in crusts with proximity to west Pacific volcanic arcs. Vernadite and CFA-related elements decrease, whereas Fe, Cu, and detrital-related elements increase with increasing water depth of crust occurrence. Cobalt, Ce, Tl, and maybe also Ti, Pb, and Pt are strongly concentrated in crusts over other metals because of oxidation reactions. Total rare earth elements (REEs) commonly vary between 0.1% and 0.3% and are derived from sea water along with other hydrogenetic elements, Co, Mn, Ni, etc. Platinum, Rh, Ir, and some Ru in crusts are also derived from sea water, whereas Pd and the remainder of the Ru derive from detrital minerals. The older parts of thick crusts were phosphatized during at least two global phosphogenic events during the Tertiary, which mobilized and redistributed elements in those parts of the crusts. 240Silicon, Fe, Al, Th, Ti, Co, Mn, Pb, and U are commonly depleted, whereas Ni, Cu, Zn, Y, REEs, Sr, and Pt are commonly enriched in phosphatized layers compared to younger nonphosphatized layers. The dominant controls on the concentration of elements in crusts include the concentration of metals in sea water and their ratios, colloid surface charge, types of complexing agents, surface area, and growth rates. Crusts act as closed systems with regard to the isotopic ratios of Be, Nd, Pb, Hf, Os, and U-series, which in part have been used to date crusts and in part used as isotopic tracers of paleoceanographic and paleoclimatic conditions. Those tracers are especially useful in delineating temporal changes in deep-ocean circulation. Research and development on the technology of mining crusts are only in their infancy. Detailed maps of crust deposits and a better understanding of small-scale seamount topography are required to design the most appropriate mining equipment.

Book chapter↗
USGS1997

The Hf isotopic composition of ferromanganese nodules and crusts and hydrothermal manganese deposits: Implications for seawater Hf

We present Hf and Pb isotopic data, and chemical compositions of the outermost layers of marine ferromanganese deposits of different types (hydrogenous and hydrothermal) with a worldwide distribution. The Hf isotopic compositions display a broad range and refine previously reported regional differences as follows: Atlantic Ocean ɛ Hf = −4to+2, Indian Ocean ɛ Hf = +2to+4, Pacific Ocean ɛ Hf = +3to+10. The most radiogenic Hf isotopic compositions in the Pacific samples are for hydrothermal manganese deposits that also have low 207 Pb 204 Pb, demonstrating that this signature reflects a contribution from hydrothermal venting of Hf leached from oceanic volcanic rocks rather than from riverine inputs, volcanic ash, or eolian dust. Hafnium concentrations in the deposits increase from 20 ppb to 20 ppm with decreasing ɛ Hf , The Hf and Pb isotopic compositions for ferromanganese crusts define an apparent mixing trend between literature values of average continental crust and MORB. The range in ɛ Hf for ferromanganese crusts is narrower than it is for 206 Pb 204 Pb compared to the differences in isotopic composition of the sources of Hf and Pb. This is consistent with Hf having a longer residence time than Pb. The concentration of Hf in ferromanganese crusts has been found to co-vary with growth rate, and inversely correlates with Hf isotopic compositions. Hf isotope ratios may be used to determine not only the source of Hf, but possibly the source of Fe and Mn. Measurements of ɛ Hf and Hf concentrations in nodule tops, bottoms and associated sediments show that the ɛ Hf of nodules is sensitive to sedimentary oxic and sub-oxic diagenetic processes and thus most nodules may not reliably reflect the isotopic composition of Hf in seawater.

Earth and Planetary Science Letters↗
USGS1997

Climate and ocean dynamics and the lead isotopic records in Pacific ferromanganese crusts

As hydrogenous iron-manganese crusts grow, at rates of millimeters per million years, they record changes in the lead isotopic composition of ambient seawater. Time-resolved lead isotopic data for cut slabs of two central Pacific iron-manganese crusts that have been growing since about 50 million years ago were measured in situ by laser ablation, multiple-collector, inductively coupled plasma mass spectrometry. The lead isotopic compositions have remained remarkably uniform over the past 30 million years, but the record of small variations corresponds with other paleoceanographic indicators of climate change, including weathering and glaciation. This implies that despite the short residence time of lead in the oceans, global mechanisms may influence lead isotopic compositions in the central Pacific, far from continental inputs, because of changes in weathering, ocean circulation, and degree of mixing. Thus lead isotopic data could be used to probe climate-driven changes in ocean circulation through time.

Science↗
USGS1996

Comparison of the partitioning behaviours of yttrium, rare earth elements, and titanium between hydrogenetic marine ferromanganese crusts and seawater

In order to evaluate details of the partitioning behaviours of Y, rare earth elements (REEs), and Ti between inorganic metal oxide surfaces and seawater, we studied the distribution of these elements in hydrogenetic marine ferromanganese (Fe-Mn) crusts from the Central Pacific Ocean. Nonphosphatized Fe-Mn crusts display shale-normalized rare earths and yttrium (REY SN ) patterns (Y inserted between Dy and Ho) that are depleted in light REEs (LREEs) and which show negative anomalies for Y sn , and positive anomalies for La SN , Eu SN , Gd SN , and in most cases, Ce sn . They show considerably smaller Y/ Ho ratios than seawater or common igneous and clastic rocks, indicating that Y and Ho are fractionated in the marine environment. Compared to P-poor crusts, REY SN patterns of phosphatized Fe-Mn crusts are similar, but yield pronounced positive Y sn anomalies, stronger positive La SN anomalies, and enrichment of the HREEs relative to the MREEs. The data suggest modification of REY during phosphatization and indicate that studies requiring primary REY distributions or isotopic ratios should be restricted to non-phosphatized (layers of) Fe-Mn crusts. Apparent bulk coefficients, K d m , describing trace metal partitioning between nonphosphatized hydrogenetic Fe-Mn crusts and seawater, are similar for Pr to Eu and decrease for Eu to Yb. Exceptionally high values of K D Ce , which are similar to those of Ti, result from oxidative scavenging of Ce and support previous suggestions that Ce (IV) is a hydroxide-dominated element in seawater. Yttrium and Gd show lower K D values than their respective neighbours in the REY series. Results of modelling the exchange equilibrium between REY dissolved in seawater and REY sorbed on hydrous Fe-Mn oxides corroborate previous studies that suggested the surface complexation of REY can be approximated by their first hydroxide binding constant. Negative “anomalies” occur for stabilities of bulk surface complexes of Gd, La, and particularly Y. The differences in inorganic surface complex stability between Y and Ho and between Gd and its REE neighbours are similar to those shown by the stabilities of complexes with aminocarboxylic acids and are significantly larger than those shown by stabilities of complexes with carboxylic acids. Hence, sorption of Y and REEs onto hydrous Fe-Mn oxides may contribute significantly to the positive Y SN and Gd SN anomalies in seawater.

Geochimica et Cosmochimica Acta↗